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Thrombosis and Haemostasis|October 6, 1997
Arg506 to Gln mutation in the factor V gene causes poor fibrinolytic response in children after venous occlusionU Nowak-Göttl, M Binder, A Dübbers, et al.
Stroke|October 7, 2000
Symptomatic ischemic stroke in full-term neonates : role of acquired and genetic prothrombotic risk factorsG Günther, R Junker, R Sträter, et al.
Blood|November 26, 1999
Lipoprotein (a) and genetic polymorphisms of clotting factor V, prothrombin, and methylenetetrahydrofolate reductase are risk factors of spontaneous ischemic stroke in childhoodU Nowak-Göttl, R Sträter, A Heinecke, et al.
Hamostaseologie|February 5, 2003
Haemophilia and thrombophilia. What do we learn about combined inheritance of both genetic variations?U Nowak-Göttl, C Escuriola, K Kurnik, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 24, 1998
Plasminogen activator inhibitor-1 4G/5G-polymorphism and factor V Q506 mutation are not associated with myocardial infarction in young menR Junker, J Heinrich, H Schulte, et al.
Circulation|August 18, 1999
Increased lipoprotein(a) is an important risk factor for venous thromboembolism in childhoodU Nowak-Göttl, R Junker, M Hartmeier, et al.
Klinische Padiatrie|January 1, 1992
[Nonparametric normal range for thrombocyte parameters in childhood]U Nowak-Göttl, E Besier, W D Kreuz, et al.
European Journal of Pediatrics|November 1, 1996
Inherited defects of the protein C anticoagulant system in childhood thrombo-embolismU Nowak-Göttl, K Auberger, U Göbel, et al.
Biomarkers in Medicine|June 6, 2018
Albumin-to-globulin ratio as an independent predictor of mortality in chronic heart failureJacek T Niedziela, Bartosz Hudzik, Bozena Szygula-Jurkiewicz, et al.
European Journal of Pediatrics|January 29, 2000
The 677T genotype of the common MTHFR thermolabile variant and fasting homocysteine in childhood venous thrombosisH G Koch, P Nabel, R Junker, et al.
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